FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CERVICAL BIOPSY INSTRUMENT
K Number: K883867
·
Decision Nov 29, 1988
Classifications
1
FEI Numbers
92
Registration Numbers
93
Same Product Code
188
Applicant Total
3
Review Days
77
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Basic Information
- Device Name
- CERVICAL BIOPSY INSTRUMENT
- K Number
- K883867
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.5470
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Applicant
- Mend Technologies, Inc.
- Date Received
- September 13, 1988
- Decision Date
- November 29, 1988
- Product Code
- HEB
- Advisory Committee
- Obstetrics/Gynecology
- Review Advisory Committee
- OB
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| HEB | Tampon, Menstrual, Unscented | FDA class 2 | Obstetrics/Gynecology |
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